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  3. 22Q11.2 DELETION SYNDROME Experts by country

22Q11.2 DELETION SYNDROME Experts

We have collected the completed list of expert related to 22Q11.2 DELETION SYNDROME using public data available on different databases.

22Q11.2 DELETION SYNDROME Experts map



If you find this map or researchers for 22Q11.2 DELETION SYNDROME useful, maybe you will be also interested in other rare diseases proffesionals like our huntington disease expert list ,or our duchenne muscular dystrophy expert list

22Q11.2 DELETION SYNDROME Experts list

Pr Koenraad DEVRIENDT

 LEUVEN. BELGIUM

  Clinical expert - Clinical geneticist - Investigator of research project

  • Research area/topic:
    Pathogenesis of congenital urological and cardiological malformations.
  • Department of Human Genetics, University Hospitals Leuven - Gasthuisberg
    Department of Human Genetics, University Hospitals Leuven - Gasthuisberg
    Department of Pediatrics, University Hospitals Leuven - Gasthuisberg
Complete Info

Dr Loydie A JEROME-MAJEWSKA

 MONTRÉAL. CANADA

  Investigator of research project

  • Research area/topic:
    The genetic basis of atypical anomalies in contiguous gene syndrome: The case of 22q11.2
  • Montreal Children's Hospital Research Institute - McGill University
    CUSM - MUHC, Glen / McGill Univeristy Health Centre - Centre Universitaire de santé McGill
  • loydie.********@***ill.ca
Complete Info

Dr Anne MARCELLINI

 MONTPELLIER. FRANCE

  Investigator of research project

  • Research area/topic:
    Becoming an adult with a developmental anomaly: barriers and facilitators
  • Université Montpellier II
  • anne.ma********@***vmontp1.fr
Complete Info

Pr Antonio BALDINI

 NAPOLI. ITALY

  Investigator of research project - Coordinator of research network

  • Research area/topic:
    Phenotypic rescue of the DiGeorge syndrome phenotype in mouse models
  • TIGEM - Telethon Institute of Genetics and Medicine
  • antonio********@***na.it
Complete Info

Dr Elizabeth ILLINGWORTH

 NAPOLI. ITALY

  Investigator of research project

  • Research area/topic:
    Identification of genes causing Schizophrenia-related behavior in a mouse model of del22q11 Syndrome
  • TIGEM - Telethon Institute of Genetics and Medicine
Complete Info

Pr Bruno DALLAPICCOLA

 ROMA. ITALY

  Coordinator of expert centre - Investigator of research project - Coordinator of research network

  • Research area/topic:
    JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot
  • IRCCS Ospedale Pediatrico Bambino Gesù - SEDE GIANICOLO
  • bruno.dal*********@***g.net
Complete Info

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All the contact information provided is based on public data available in orpha.net.